• Macromolecular Research
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• v.17 no.7
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• pp.483-490
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• 2009

Stable poly(styrene-co-divinylbenzene) [P(St-co-DVB)] micro spheres with narrow size distribution were synthesized in the presence of 2,2'-azobis(2,4-dimethyl valeronitrile) (V-65) and co-initiator in an acetone/water mixture in the precipitation polymerization at $53^{\circ}C$ for 24 h. Potassium peroxodisulfate (KPS), ammonium peroxodisulfate (APS) and sodium peroxodisulfate (NaPS) were used as co-initiators. The optimum ratio of acetone to water for the formation of a narrow distribution of P(St-co-DVB) particles was 49:11 (g/g). The optimum co-initiator compositions for narrow distribution were 9:1 (g/g) for V-65 to KPS, 11:1 for V-65 to APS and 6:1 for V-65 to NaPS. The yield for these compositions was $54{\sim}57%$ and the largest particle size was obtained with the lowest zeta-potential and CV values. From the XPS measurements, the charge density was increased but the zeta potential decreased with increasing sulfur content, implying that the sulfate group provides the electrostatic stabilization on the particle surface. This suggested that the self-crosslinking between styrene and DVB, the electrostatic stabilization of initiators, and the balanced hydrophobic and hydrophilic properties of the solvents are responsible for the formation of stable P(St-co-DVB) spherical particles with narrow size distribution.

• Macromolecular Research
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• v.12 no.5
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• pp.519-527
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• 2004

Stable poly(methyl methacrylate-co-divinylbenzene) (poly(MMA-co-DVB)) microspheres were prepared by precipitation polymerization using acetonitrile as the main medium under various polymerization conditions, including modifications of the agitation speed, monomer and initiator concentrations, DVB content in the monomer mixture, and the use of various cosolvents. Gentle agitation was required to obtain smooth spherical particles. The individually stable microspheres were obtained at monomer concentrations of up to 15 vol% in an acetonitrile medium. The number-average diameter increased linearly with respect to increases in the monomer and initiator concentrations. We found, however, that the uniformity of the microspheres was independent of the variation of the polymerization ingredients because nuclei formation was solely influenced by the crosslinking reaction of the monomers. We obtained higher yields for the polymerization at higher concentrations of monomer and initiator. The concentration of DVB in the monomer mixture composition played an important role in determining not only the size of the microspheres but also the yield of the polymerization. In addition, although we employed various cosolvents as the polymerization medium, we found that acetonitrile/2-methoxyethanol was the only system that provided spherical particles without coagulation. This finding indicates that the precipitation polymerization is strongly dependent on the solvent used as the medium.

• 한국정보디스플레이학회:학술대회논문집
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• 2004.08a
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• pp.1208-1211
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• 2004

When irradiated with visible light in HPDLC, photoinitiator and coinitiator produce a radical for photopolymerization. According to the kinds of photoinitiator and coinitiator, quantity and rate of produced a radical is different. It is influence on photopolymerization rate relate on diffraction efficiency. Thus, this paper is about the effect of photoinitiator/coinitiator combinations in terms of diffraction efficiency and real-time first order diffraction efficiency.

• Journal of Photoscience
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• v.5 no.2
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• pp.63-67
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• 1998

New photoinitiator systems of dimethylphenacylsulfonium butyltnphenylborate (DMPSB) as a donor-acceptor initiator and styryl dyes have been investigated for free radical polymerization of an acrylate with visible lasers (488, 514 and 647 nm). DMPSB was able to be sensitized by many styryl dyes. When polymerized with pentaerythrithol triacrylate, the sensitivity value of the photosensitive layer containing DMPSB was higher than that of an tetrabutylammonium butyltnphenylborate (TBAB) as an electron donating initiator or a dimethylphenacylsulfonium tetrafiuoroborate (DMPS) as an electron accepting initiator. The sensitivity values of the photosensitive layer containing the photoinitiator systems had a close relation to the free energy changes between the excited singlet styryl dyes and DMPSB.

• Transactions of the Korean Society of Automotive Engineers
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• v.18 no.3
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• pp.69-73
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• 2010

The melt grafting of unsaturated silanes onto polypropylene (PP) in a twin-screw extruder and crosslinking in hot water were studied to enhance impact strength of polypropylene. The influence of grafting formulations on the melt flow rates of grafted PP and the gel percentages of crosslinked PP was investigated. 3-methacryloylpropyltrimethoxysilane (VMMS) unsaturated silane monomer was used. Benzoyl peroxide, (BPO) and Dicumyl peroxide (DCP) were used as an initiator. When benzoyl peroxide (BPO) was used as an initiator, higher gel percentage and impact strength than those of DCP has been observed. The maximum impact strength was obtained with 0.7 phr of BPO and 2phr of VMMS. The value is 8.7 kgf-cm/cm and it is on a parity with the value of with 20 phr of EOR mixed to PP.

• Elastomers and Composites
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• v.28 no.3
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• pp.191-197
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• 1993

The graft copolymerization of methyl methacrylate(MMA) onto natural rubber latex(NRL) initiated by t-butyl hydroperoxide(t-BHPO) was investigated in aquous medium. The grafting percentage, grafting efficiency and total conversion were observed in various reaction conditions such as monomer, initiator and emulsifier concentration, reaction temperature, reaction time and agitation speed. The optimum conditions for the graft copolymerization onto natural rubber latex were as follows ; At given monomer concentration of $3{\times}10^{-2}mole/l$, the maximum grafting percentage was appeared in the case of grading in initiator concentration of $4{\times}10^{-2}mo1e/l$ and emulsifier concentration of 0.2wt.% at $40^{\circ}C$ for 5hrs.

• Polymer(Korea)
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• v.38 no.1
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• pp.16-23
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• 2014

A novel poly(AM-DMDAAC)/MMT superabsorbent nanocomposites are prepared by radical polymerization using ammonium persulfate (APS) and anhydrous sodium sulfite as a free radical initiator and N,N-methylene bisacrylamide (MBA) as a crosslinker. In this paper, an optimization study on the synthesis of superabsorbent nanocomposites is carried out. Orthogonal array experiment indicates that the optimized conditions is acrylamide (AM) content 23 wt%, diallyl dimethyl ammonium chloride (DMDAAAC) content 6 wt%, montmorillonite (MMT) content 4 wt%, initiator content 0.2 wt% and crosslinker content 0.02 wt%. Under the optimization syntheses conditions concluded, the maximum water absorbency in distilled water is $659.53g{\cdot}g^{-1}$ and in 2 wt% sodium chloride solution is $116.25g{\cdot}g^{-1}$. Compared with the range values of different factors ($R_j$), the order of significance factors in distilled water is C (MMT) > B (DMDAAC) > A (AM) > D (crosslinker) > E (initiator). MMT is intercalated during polymerization reaction and a nanocomposite structure is formed as shown by TEM analysis and XRD analysis.

• Macromolecular Research
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• v.16 no.2
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• pp.120-127
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• 2008

Glycidyl methacrylate linked poly(dimethylsiloxane) (GMA-PDMS) was synthesized and used as a stabilizer for the dispersion polymerization of methyl methacrylate (MMA) in supercritical $CO_2$. This study examined the effect of the concentrations of the stabilizer, 2,2'-azobisisobutyronitrile (AIBN) initiator, and MMA on the yield, molecular weight, and morphology of the poly(methyl methacrylate) (PMMA) product. PMMA was obtained in 94,6% yield using only 0,87 wt% GMA-PDMS, When the AIBN concentration was increased from 025 to 1.06 wt%, the molecular weight and particle size of the PMMA decreased from 56,600 to 21,600 and from 4.1 to $2.7{\mu}m$, whereas the particle size distribution increased from 1.3 to 1.9. The $M_n$ of the PMMA product ranged from 41,600 and 55,800 under typical polymerization conditions. The PMMA particle diameter ranged from 1.8 to $11.0{\mu}m$ and the particle size distribution ranged from 1.4 to 1.8.

• Polymer(Korea)
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• v.32 no.2
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• pp.116-124
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• 2008

A commercialized biobased and biodegradable poly(lactic acid)(PLA) containing the functional monomer of glycidyl methacrylate (GMA) was chemically modified using reactive extrusion to enhance its melt strength. Modified PLAs were prepared with various contents of GMA and initiator, and were characterized by observing their gel fraction, thermal properties, melt viscoelasticity and biodegradability. The complex viscosity and storage modulus of chemically modified PLA with the initiator alone was increased by addition of initiator and were more increased in the presence of GMA. There was a optimum content of GMA showing the maximum complex viscosity with the amount of initiator. The biodegradebility of modified PLA was slightly decreased by addition of GMA.

• Journal of the Korean Chemical Society
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• v.23 no.6
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• pp.402-411
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• 1979

The synthesis of pyrrolidone-N-sulfonyl chloride has been carried out by the reaction of pyrrolidone with sulfuryl chloride in benzene. It was attempted to study the catalytic effect of pyrroldone-N-sulfonyl chloride as an initiator for anionic polymerization of pyrrolidone. It was found that as a concentration of initiator decreased, inherent viscosity of the resulting polymer increased up to 1.8 dl/g. The highest rate of polymerization and equilibrium conversion was observed when mole ratio of PNSC to KOH was 0.25. In general, the observed value of polymerization and equilibrium conversion in circumstances using PNSC/KOH catalysis system were higher than using $CO_2$/KOH catalysis system.